Osborn Group, Inc.
FDA Regulatory Profile
Osborn Group, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 19, 2000.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K002156 | APPRAISE URINE MICROALBUMIN COLLECTION KIT | December 19, 2000 |
| K993787 | APPRAISE-CARDIO SAMPLE COLLECTION KIT | April 14, 2000 |
| K990899 | HEMOCHEK-A1C SAMPLE COLLECTION KIT | December 21, 1999 |
| K991800 | HEMOCHEK URINE COLLECTION KIT | September 24, 1999 |